Sustaining benefits of nutritional therapy in young adults with phenylketonuria - A 2 year prospective study

INTRODUCTION: Phenylketonuria (PKU) is an inborn error of metabolism, which is caused by a deficiency in the enzyme phenylalanine hydroxylase (PAH). Life-long Phe-free diet impairs quality of life, especially in adolescents and young adults which take responsibility over their diet and therapy from...

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Detalles Bibliográficos
Autor principal: Krämer, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026618/
https://www.ncbi.nlm.nih.gov/pubmed/32099818
http://dx.doi.org/10.1016/j.ymgmr.2020.100573

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026618/
https://www.ncbi.nlm.nih.gov/pubmed/32099818
http://dx.doi.org/10.1016/j.ymgmr.2020.100573

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